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Comparison of Clinical Characteristics and Predictors of Mortality between Direct and Indirect ARDS
Background and Objectives: Acute Respiratory Distress Syndrome (ARDS) is a heterogeneous syndrome that encompasses lung injury from a direct pulmonary or indirect systemic insult. Studies have shown that direct and indirect ARDS differ in their pathophysiologic process. In this study, we aimed to co...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9697068/ https://www.ncbi.nlm.nih.gov/pubmed/36363520 http://dx.doi.org/10.3390/medicina58111563 |
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author | Tang, Wen Tang, Rui Zhao, Yan Peng, Junnan Wang, Daoxin |
author_facet | Tang, Wen Tang, Rui Zhao, Yan Peng, Junnan Wang, Daoxin |
author_sort | Tang, Wen |
collection | PubMed |
description | Background and Objectives: Acute Respiratory Distress Syndrome (ARDS) is a heterogeneous syndrome that encompasses lung injury from a direct pulmonary or indirect systemic insult. Studies have shown that direct and indirect ARDS differ in their pathophysiologic process. In this study, we aimed to compare the different clinical characteristics and predictors of 28-day mortality between direct and indirect ARDS. Materials and Methods: The data of 1291 ARDS patients from September 2012 to December 2021 at the Second Affiliated Hospital of Chongqing Medical University were reviewed. We enrolled 451 ARDS patients in our study through inclusion and exclusion criteria. According to the risk factors, each patient was divided into direct (n = 239) or indirect (n = 212) ARDS groups. The primary outcome was 28-day mortality. Results: The patients with direct ARDS were more likely to be older (p < 0.001) and male (p = 0.009) and have more comorbidity (p < 0.05) and higher 28-day mortality (p < 0.001) than those with indirect ARDS. Age and multiple organ dysfunction syndrome (MODS) were predictors of 28-day mortality in the direct ARDS group, while age, MODS, creatinine, prothrombin time (PT), and oxygenation index (OI) were independent predictors of 28-day mortality in the indirect ARDS group. Creatinine, PT, and OI have interactions with ARDS types (all p < 0.01). Conclusions: The patients with direct ARDS were more likely to be older and male and have worse conditions and prognoses than those with indirect ARDS. Creatinine, PT, and OI were predictors of 28-day mortality only in the indirect ARDS group. The differences between direct and indirect ARDS suggest the need for different management strategies of ARDS. |
format | Online Article Text |
id | pubmed-9697068 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-96970682022-11-26 Comparison of Clinical Characteristics and Predictors of Mortality between Direct and Indirect ARDS Tang, Wen Tang, Rui Zhao, Yan Peng, Junnan Wang, Daoxin Medicina (Kaunas) Article Background and Objectives: Acute Respiratory Distress Syndrome (ARDS) is a heterogeneous syndrome that encompasses lung injury from a direct pulmonary or indirect systemic insult. Studies have shown that direct and indirect ARDS differ in their pathophysiologic process. In this study, we aimed to compare the different clinical characteristics and predictors of 28-day mortality between direct and indirect ARDS. Materials and Methods: The data of 1291 ARDS patients from September 2012 to December 2021 at the Second Affiliated Hospital of Chongqing Medical University were reviewed. We enrolled 451 ARDS patients in our study through inclusion and exclusion criteria. According to the risk factors, each patient was divided into direct (n = 239) or indirect (n = 212) ARDS groups. The primary outcome was 28-day mortality. Results: The patients with direct ARDS were more likely to be older (p < 0.001) and male (p = 0.009) and have more comorbidity (p < 0.05) and higher 28-day mortality (p < 0.001) than those with indirect ARDS. Age and multiple organ dysfunction syndrome (MODS) were predictors of 28-day mortality in the direct ARDS group, while age, MODS, creatinine, prothrombin time (PT), and oxygenation index (OI) were independent predictors of 28-day mortality in the indirect ARDS group. Creatinine, PT, and OI have interactions with ARDS types (all p < 0.01). Conclusions: The patients with direct ARDS were more likely to be older and male and have worse conditions and prognoses than those with indirect ARDS. Creatinine, PT, and OI were predictors of 28-day mortality only in the indirect ARDS group. The differences between direct and indirect ARDS suggest the need for different management strategies of ARDS. MDPI 2022-10-30 /pmc/articles/PMC9697068/ /pubmed/36363520 http://dx.doi.org/10.3390/medicina58111563 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Tang, Wen Tang, Rui Zhao, Yan Peng, Junnan Wang, Daoxin Comparison of Clinical Characteristics and Predictors of Mortality between Direct and Indirect ARDS |
title | Comparison of Clinical Characteristics and Predictors of Mortality between Direct and Indirect ARDS |
title_full | Comparison of Clinical Characteristics and Predictors of Mortality between Direct and Indirect ARDS |
title_fullStr | Comparison of Clinical Characteristics and Predictors of Mortality between Direct and Indirect ARDS |
title_full_unstemmed | Comparison of Clinical Characteristics and Predictors of Mortality between Direct and Indirect ARDS |
title_short | Comparison of Clinical Characteristics and Predictors of Mortality between Direct and Indirect ARDS |
title_sort | comparison of clinical characteristics and predictors of mortality between direct and indirect ards |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9697068/ https://www.ncbi.nlm.nih.gov/pubmed/36363520 http://dx.doi.org/10.3390/medicina58111563 |
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